Job Summary
A global group of pharmaceutical companies needs applicants for an opening for a Remote Medical Writing Associate Director in Ridgefield.
Candidates will be responsible for the following:
- Contributing to development of global regulatory documentation strategy
- Coordinating medical writing/regulatory submission progress
- Writing or co-ordinating writing and reviews of clinical trial reports
Qualifications for this position include:
- 6-8 years of experience in medical writing
- Evidence of the skills necessary to manage submissions
- Evidence of the skills to manage a group of 0-5 medical writers
- Must have relevant medical/scientific knowledge
- Project management skills
- Knowledge of drug development and regulatory requirements
